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1.
Cereb Cortex ; 18(2): 301-14, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17615251

ABSTRACT

The rat auditory cortex is divided anatomically into several areas, but little is known about the functional differences in information processing between these areas. To determine the filter properties of rat posterior auditory field (PAF) neurons, we compared neurophysiological responses to simple tones, frequency modulated (FM) sweeps, and amplitude modulated noise and tones with responses of primary auditory cortex (A1) neurons. PAF neurons have excitatory receptive fields that are on average 65% broader than A1 neurons. The broader receptive fields of PAF neurons result in responses to narrow and broadband inputs that are stronger than A1. In contrast to A1, we found little evidence for an orderly topographic gradient in PAF based on frequency. These neurons exhibit latencies that are twice as long as A1. In response to modulated tones and noise, PAF neurons adapt to repeated stimuli at significantly slower rates. Unlike A1, neurons in PAF rarely exhibit facilitation to rapidly repeated sounds. Neurons in PAF do not exhibit strong selectivity for rate or direction of narrowband one octave FM sweeps. These results indicate that PAF, like nonprimary visual fields, processes sensory information on larger spectral and longer temporal scales than primary cortex.


Subject(s)
Acoustic Stimulation/methods , Auditory Cortex/physiology , Evoked Potentials, Auditory/physiology , Nerve Net/physiology , Neural Pathways/physiology , Neurons, Afferent/physiology , Pitch Perception/physiology , Animals , Female , Rats , Rats, Sprague-Dawley
2.
J Neurophysiol ; 98(1): 253-65, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17460101

ABSTRACT

Classical conditioning paradigms have been shown to cause frequency-specific plasticity in both primary and secondary cortical areas. Previous research demonstrated that repeated pairing of nucleus basalis (NB) stimulation with a tone results in plasticity in primary auditory cortex (A1), mimicking the changes observed after classical conditioning. However, few studies have documented the effects of similar paradigms in secondary cortical areas. The purpose of this study was to quantify plasticity in the posterior auditory field (PAF) of the rat after NB stimulation paired with a high-frequency tone. NB-tone pairing increased the frequency selectivity of PAF sites activated by the paired tone. This frequency-specific receptive field size narrowing led to a reorganization of PAF such that responses to low- and mid-frequency tones were reduced by 40%. Plasticity in A1 was consistent with previous studies -- pairing a high-frequency tone with NB stimulation expanded the high-frequency region of the frequency map. Receptive field sizes did not change, but characteristic frequencies in A1 were shifted after NB-tone pairing. These results demonstrate that experience-dependent plasticity can take different forms in both A1 and secondary auditory cortex.


Subject(s)
Auditory Cortex/cytology , Basal Nucleus of Meynert/physiology , Brain Mapping , Neuronal Plasticity/physiology , Neurons/physiology , Action Potentials/physiology , Afferent Pathways/physiology , Animals , Dose-Response Relationship, Radiation , Electric Stimulation/methods , Female , Rats , Rats, Sprague-Dawley , Spectrum Analysis
3.
Prog Brain Res ; 157: 111-122, 2006.
Article in English | MEDLINE | ID: mdl-17167905

ABSTRACT

The brain is constantly adapting to environmental and endogenous changes (including injury) that occur at every stage of life. The mechanisms that regulate neural plasticity have been refined over millions of years. Motivation and sensory experience directly shape the rewiring that makes learning and neurological recovery possible. Guiding neural reorganization in a manner that facilitates recovery of function is a primary goal of neurological rehabilitation. As the rules that govern neural plasticity become better understood, it will be possible to manipulate the sensory and motor experience of patients to induce specific forms of plasticity. This review summarizes our current knowledge regarding factors that regulate cortical plasticity, illustrates specific forms of reorganization induced by control of each factor, and suggests how to exploit these factors for clinical benefit.


Subject(s)
Brain Injuries/rehabilitation , Cerebral Cortex/physiology , Neuronal Plasticity/physiology , Humans , Neurotransmitter Agents/metabolism , Neurotransmitter Agents/physiology , Sensation/physiology
4.
J Neurophysiol ; 94(5): 3590-600, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16093336

ABSTRACT

Temporal features are important for the identification of natural sounds. Earlier studies have shown that cortical processing of temporal information can be altered by long-term experience with modulated sounds. In a previous study, we observed that environmental enrichment dramatically increased the response of cortical neurons to single tone and noise burst stimuli in both awake and anesthetized rats. Here, we evaluate how enrichment influences temporal information processing in the auditory cortex. We recorded responses to repeated tones and noise bursts in awake rats using epidural evoked potentials and in anesthetized rats using microelectrodes. Enrichment increased the response of cortical neurons to stimuli presented at slow rates and decreased the response to stimuli presented at fast rates relative to controls. Our observation that enrichment substantially increased response strength and forward masking is consistent with earlier reports that long-term potentiation of cortical synapses is associated with increased paired-pulse depression. Enrichment also increased response synchronization at slow rates and decreased synchronization at fast rates. Paired-pulse depression increased within days of environmental enrichment and was restored to normal levels after return to standard housing conditions. These results are relevant to several clinical disorders characterized by abnormal gating of sensory information, including autism, schizophrenia, and dyslexia.


Subject(s)
Acoustic Stimulation/methods , Auditory Cortex/physiology , Environment , Evoked Potentials, Auditory/physiology , Long-Term Potentiation/physiology , Neurons/physiology , Pitch Perception/physiology , Action Potentials/physiology , Adaptation, Physiological/physiology , Animals , Female , Neural Inhibition/physiology , Neuronal Plasticity/physiology , Rats , Rats, Sprague-Dawley
5.
Hear Res ; 203(1-2): 10-20, 2005 May.
Article in English | MEDLINE | ID: mdl-15855025

ABSTRACT

Correlation-based synaptic plasticity provides a potential cellular mechanism for learning and memory. Studies in the visual and somatosensory systems have shown that behavioral and surgical manipulation of sensory inputs leads to changes in cortical organization that are consistent with the operation of these learning rules. In this study, we examine how the organization of primary auditory cortex (A1) is altered by tones designed to decrease the average input correlation across the frequency map. After one month of separately pairing nucleus basalis stimulation with 2 and 14 kHz tones, a greater proportion of A1 neurons responded to frequencies below 2 kHz and above 14 kHz. Despite the expanded representation of these tones, cortical excitability was specifically reduced in the high and low frequency regions of A1, as evidenced by increased neural thresholds and decreased response strength. In contrast, in the frequency region between the two paired tones, driven rates were unaffected and spontaneous firing rate was increased. Neural response latencies were increased across the frequency map when nucleus basalis stimulation was associated with asynchronous activation of the high and low frequency regions of A1. This set of changes did not occur when pulsed noise bursts were paired with nucleus basalis stimulation. These results are consistent with earlier observations that sensory input statistics can shape cortical map organization and spike timing.


Subject(s)
Acoustic Stimulation/methods , Auditory Cortex/physiology , Neuronal Plasticity , Action Potentials , Animals , Basal Nucleus of Meynert/physiology , Brain Mapping , Differential Threshold , Electric Stimulation , Electrophysiology , Rats , Rats, Sprague-Dawley , Reaction Time
6.
Exp Brain Res ; 162(4): 417-27, 2005 May.
Article in English | MEDLINE | ID: mdl-15616812

ABSTRACT

The mammalian auditory system evolved to extract meaningful information from complex acoustic environments. Spectrotemporal selectivity of auditory neurons provides a potential mechanism to represent natural sounds. Experience-dependent plasticity mechanisms can remodel the spectrotemporal selectivity of neurons in primary auditory cortex (A1). Electrical stimulation of the cholinergic nucleus basalis (NB) enables plasticity in A1 that parallels natural learning and is specific to acoustic features associated with NB activity. In this study, we used NB stimulation to explore how cortical networks reorganize after experience with frequency-modulated (FM) sweeps, and how background stimuli contribute to spectrotemporal plasticity in rat auditory cortex. Pairing an 8-4 kHz FM sweep with NB stimulation 300 times per day for 20 days decreased tone thresholds, frequency selectivity, and response latency of A1 neurons in the region of the tonotopic map activated by the sound. In an attempt to modify neuronal response properties across all of A1 the same NB activation was paired in a second group of rats with five downward FM sweeps, each spanning a different octave. No changes in FM selectivity or receptive field (RF) structure were observed when the neural activation was distributed across the cortical surface. However, the addition of unpaired background sweeps of different rates or direction was sufficient to alter RF characteristics across the tonotopic map in a third group of rats. These results extend earlier observations that cortical neurons can develop stimulus specific plasticity and indicate that background conditions can strongly influence cortical plasticity.


Subject(s)
Auditory Cortex/physiopathology , Auditory Perception/physiology , Basal Nucleus of Meynert/physiology , Cholinergic Fibers/physiology , Neuronal Plasticity/physiology , Acoustic Stimulation , Animals , Auditory Threshold/physiology , Brain Mapping , Electric Stimulation , Female , Neurons/physiology , Pitch Discrimination/physiology , Rats , Rats, Sprague-Dawley , Reaction Time/physiology
7.
J Neurophysiol ; 92(1): 73-82, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15014105

ABSTRACT

Over the last 50 yr, environmental enrichment has been shown to generate more than a dozen changes in brain anatomy. The consequences of these physical changes on information processing have not been well studied. In this study, rats were housed in enriched or standard conditions either prior to or after reaching sexual maturity. Evoked potentials from awake rats and extracellular recordings from anesthetized rats were used to document responses of auditory cortex neurons. This report details several significant, new findings about the influence of housing conditions on the responses of rat auditory cortex neurons. First, enrichment dramatically increases the strength of auditory cortex responses. Tone-evoked potentials of enriched rats, for example, were more than twice the amplitude of rats raised in standard laboratory conditions. Second, cortical responses of both young and adult animals benefit from exposure to an enriched environment and are degraded by exposure to an impoverished environment. Third, housing condition resulted in rapid remodeling of cortical responses in <2 wk. Fourth, recordings made under anesthesia indicate that enrichment increases the number of neurons activated by any sound. This finding shows that the evoked potential plasticity documented in awake rats was not due to differences in behavioral state. Finally, enrichment made primary auditory cortex (A1) neurons more sensitive to quiet sounds, more selective for tone frequency, and altered their response latencies. These experiments provide the first evidence of physiologic changes in auditory cortex processing resulting from generalized environmental enrichment.


Subject(s)
Auditory Cortex/physiology , Auditory Threshold/physiology , Housing, Animal , Neurons/physiology , Reaction Time/physiology , Acoustic Stimulation/methods , Action Potentials/physiology , Animals , Female , Rats , Rats, Sprague-Dawley
8.
Biol Cybern ; 87(5-6): 333-43, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12461624

ABSTRACT

Sensory experience alters the functional organization of cortical networks. Previous studies using behavioral training motivated by aversive or rewarding stimuli have demonstrated that cortical plasticity is specific to salient inputs in the sensory environment. Sensory experience associated with electrical activation of the basal forebrain (BasF) generates similar input specific plasticity. By directly engaging plasticity mechanisms and avoiding extensive behavioral training, BasF stimulation makes it possible to efficiently explore how specific sensory features contribute to cortical plasticity. This review summarizes our observations that cortical networks employ a variety of strategies to improve the representation of the sensory environment. Different combinations of receptive-field, temporal, and spectrotemporal plasticity were generated in primary auditory cortex neurons depending on the pitch, modulation rate, and order of sounds paired with BasF stimulation. Simple tones led to map expansion, while modulated tones altered the maximum cortical following rate. Exposure to complex acoustic sequences led to the development of combination-sensitive responses. This remodeling of cortical response characteristics may reflect changes in intrinsic cellular mechanisms, synaptic efficacy, and local neuronal connectivity. The intricate relationship between the pattern of sensory activation and cortical plasticity suggests that network-level rules alter the functional organization of the cortex to generate the most behaviorally useful representation of the sensory environment.


Subject(s)
Cerebral Cortex/physiology , Nerve Net/physiology , Neuronal Plasticity/physiology , Sensation/physiology , Acetylcholine/metabolism , Animals , Brain Mapping , Cerebral Cortex/anatomy & histology , Cerebral Cortex/cytology , Neurons/physiology , Reaction Time/physiology , Time Factors
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